Note : Les descriptions sont présentées dans la langue officielle dans laquelle elles ont été soumises.
37
Thls lnvention relates to a dentifrlce preparation. hlore
particularly, it relates to a dentifric0 preparation which has a
rheologically smooth surface appearallce.
Dentifrices containing polishing materials including
certain siliceous polishing agents having a refractive index of
about 1.~ 7 have desirable cosmetic effects in the clean-
ing and polishing of tooth surfaces. The dentifrices are also
compatible wi~h many hygenic and prophylactic agents such as
cariostatic compounds which provide fluoride. Further~ they may
be used to formulate visually clear ~that is, translucent or
transparent) dentifrice preparations. The dentifrice formulae may
also be modified by including elevated amounts of water and/or
opacifying agents in order to render the dentifrices opaque.
Dentifrice preparations containing such siliceous polish-
ing agents, may appear to the beholder to be rheologically some-
what deformed in that lumps appear to be present when an elevated
amount of water ~say, at least about 35% by weight) is present.
This is particularly so when the dentifrice is opaque so that only
the surface is visible. Lumping becomes a particular problem when
the preparation has been stored under cool temperature conditions.
These lumps are quite soft and do not negatively affect extrusion
of the dentifrice from its package. Further, they are not felt
when the dentifrice is brushed on the teeth and dispersed in the
oral cavity. Nevertheless, due to their appearance, the lumps
~'
may dissuade some potential customers from using what is in
reality a hygenically desirable and beneFicial dentifrice pre-
paration.
The problem of soft lump formation particularly occurs
when the opaque dentifrice contains at least abowt 35% by weight
of water and sodium alkyl sulphate having a broad distribution
of alkyl groups containing 10 - 18 carbon atoms. The reference
to "water" refers to water whlch is free of association with a
particular ingredient of the dentifrice such as water present to
dissolve sorbitol.
It is an advantage of this invention that a dentifrice
preparation is provided which is smooth without substantial
rheological deformation. Further advantages will be apparent
from consideration of the following disclosure.
In accordance with the present in~ention there is
provided an opaque dentifrice preparation comprising a liquid
vehicle which contains at least about 35% by weight of water,
up to about 10% by weight of a gelling agent5 and about 10 - 50%
by weight of a polishing material at least a major portion of
which is a siliceous polishing material having an empirical SiO2
content of at least 70%, a particle size in the range from 1 to 35
microns, substantially amorphous x-ray structure and a refractive
index of about 1.40 - 1.~7, about 0.1 - 5% by weight of a surface
active agent containing sodium alkyl sulphate wherein the alkyl
group contains lO - 18 carbon atoms, with about 40 - 70% of the
alkyl groups being Cl2 and about 0.1 - 15% by weight of a water-
soluble~ orally acceptable salt of an alkylene diamine tetramethylene
phosphonic acid, wherein the alkylene group contains 1 - 10 carbon
atoms.
-- 2 --
In British Pa~en~s l,5~9,690 and l,599~689 (corresponding to
.S. Patents 4,264,580 and 4,301,143) grain Eormation
at low ~emperatures (e.g. about -7 to 7C) in denti~rLces
containing calcium carbonate polishing agent and sodium alkyl
sulphate with a broad distribution about C10-Cl~ alkyl groups
is reduced by employing an alkali metal pyrophosphate or an
anionic phosphate ester. Alkylene diamine Letramethyl phosphonic
acid salt was not used~ Indeed, it is known from British
Patent 1,344,185 that it is pre~erred not to use calcium
carbonate in a dentifrice together with alkylene diamine tetra-
phosphonic acid salt.
In the present invention it was found that soft lumps which
form, particularly upon aging at low te~perature such as about
-7 to 7C could be reduced in a dentifrice containing a polishing
material based on sodium aluminosilicate or silica containing
combined alumina, an unassociated water level of at least about
35% by weight of the dentifrice and a surface active material
including sodium alkyl sulphate having a broad alkyl distribution
of about 10 to 18 carbon atoms by including Cl-10 alkylene
diamine tetraphosphonic acid alkali metal salt in the dentifrice.
From the point of view of rheological appearance, soft
lump formation is even more serious than graininess. A dentifrice
is of poor appearance when deformed by lumps.
The proportion of the polishing agent of high silica content
is in the ran8e from 5% to 50% of the dentifrice, preEerably
from 10% to 30%, such as from 15% to 25%. One abrasive is an
amorphous alkali metal or alkaline earth metal aluminosilicate
(that is, silica containing combined alumina having~a refractive
index of from 1.40 to 1.47,such as 1.44 to 1.47,and containing
at least 70% silica, up to 10%, typically about 0.1-10~.
alumina, up to 20% of moisture and up to lO~o of sodium oxide.
Typically, this material has a particle size in the range from
1 to 35 microns, preferably from 2 to 20 microns, e.g. 2 to 4
microns. The preferred moisture content is Erom 10% to 20%
measured by ignition at 1000 C. and the typical content of
sodium oxide is from 0.5,'0 to 10%. Generally, ~he pnlLshing
agent has a loose bulk density of up to 0.2 g/cc, such as Erom
0.07 to 0.12 g/cc. Another suitable type of polish:Lng agent
is porous amorphous siliclc anhydride having an average par-ticle
size preferably below 20 microns and above 1 micron, a surface
area of at least 200 m2/g, preferably at least 300 m2/g, and
bulk density of at least 0.15 g/cm3, preferably at least 0.30
g/cm3, such as a dehydrated silica hydrogel (i.e. a xerogel),
preferably of the well known regular density or intermediate
density type. Examples of such amorphous siliclc anhydride
polishing agents are "Syloid 63", Syloid 72", and Syloid 74"
~SYLOID is a trade mark) which are described in "The Davison
Family of Syloid Silicas" published by their manufacturers,
Grace, Davison Chemical Company. "Santocel 100" of Monsanto
~SANTOCEL is a trade mark~, is also a suitable dental abrasive.
"Syloid 72" has an average Particle size of about 4 microns,
a surface area of about 340 m2/g and a bulk density of about
1.77 g/cm3. For "Syloid 63" the corresponding figures are
about 9 microns, about 675 m2/g and about 0.4 g/cm3. A grade
of "Santocel 100" has a surface area of about 239 m2/g
and a bulk density of about 0.24 g/cm3. These amorphous silicic
anhydrides may be used singly or in mlxtures.
When the siliceous polishing agent amounts to at least
about 10% by weight of the dentifrice, it may be the only
polishing agent present. If desired the siliceous pollshing
agent may be present in major amount (at least half of the
polishing material) with regard to a further polishing agent or
polishing agent mixture. The further polishing agent may be
dentally acceptable polishing agents such as calcined alumina,
alpha-alumina trihydrate, dicalcium phosphate dihydrateg anhydrous
dicalcium phosphate, insoluble sodlum metaphosphate, calcium
carbonate and the like, including mixture thereof. Calcined
alumina is preferred. The further polishing agent, ~including
mixtures thereof) is typically present in an amount
of about 5-20% not exceeding the amount of siliceous pollshlng
agent. The further polishing ~naterial deepens the opa~ueness
o the dentirice.
~ he surface active agent includes sodium alkyl sulphate
having a broad distribution of alkyl groups containlng 10-18
carbon atoms.
Sodium lauryl sulphate has long been used in dentiErice
compositions but it has generally been used as a "narrow cut"
material in which at least 90~, even 99%, of the alkyl groups
are Cl~. Dental creams containing siliceous polishlng agent a~d
"narrow cut" sodium lauryl sulphate often do not become lumpy
even upon aging at low temperatures. Commercially available
grades of "narrow cut" sodium lauryl sulphate include
*
Empicol 0045 available from Marchon Division of ~lbright & Wilson,
Texapon K 1296 available from ~enkel and Cie. and Alfol 12
available from Conoco.
When sodium alkyl sulphate of broader alkyl distribution
is employed, the problem of 1umping upon aging at low temperature
can be recognized. A particular sodium lauryl sulphate employed
for the present invention contains about 3% ClO; 56% C12;
21% C14; 9% Cl6; and 11% C18 alkyl groups and is commercially
available in the form of needles as Empicol "LZV" from Marchon
Division of Albright and Wilson, Whitehaven, England. Further
broad cut grades of sodium alkyl sulphate which may be employed
are Tensopol SP ACL7 from Tensia S, A., Leige, Belgium and
Texapon ZHC from Henkel and Cie., Dusseldorf, West Germany.
Such grades of sodium alkyl sulphate include in their alkyl
distribution about 40 to 70% C12. More particularly,
* Trade Mark
~hey typlcally have an aLkyl distribution oE about 1 to ~ C10;
40 to 70~ C12, 13 to 30% C14; 5 to 16% C16, and 0-23% C18.
The alkyl groups are substantially straight chain (normal).
The sodium alkyl sulphate may be pLepared by means known
in the art to give a produc~ with broad alkyl distribution.
"Narrow cut" sodium lauryl sulfat~ would be prepared from the
broader cut material by fractional distillation and recrystallisa-
tion.
In addition to sodium alkyl sulphate of broad alkyl
distribution, the dent-lfrice optionally may include an
additional surface active agent. Such agents may include
anionic materials, for instance, water-soluble salts of
higher fatty acid monoglyceride monosulphate (e.g. sodium
coconut fatty acid monoglyceride monosulphate), alkyl aryl
sulphonate (e.g. sodium dodecyl benzene sulphonate), higher
fatty acid esters of 1,2-dihydroxy propane sulphate (e.g.
sodium coconut fatty acid ester of 1,2-dlhydroxypropane
sulphonate) etc.
A nonionic or ampholytic surface active agent may also
be present, such agents including nonionic agents such as
sorbitan monosteàrate with approximately 20 moles
of ethylene oxide, condensates of ethylene oxide with propylene
oxide (available under the trademark "Pluronics")
and amphoteric agents such as quaternized imidazole derivatives
which are available under the trademark "~iranol" such as
Miranol C2~1. It is preEerred that the total amount o~
surface active agent does not exceecl about 5~ by wei~ht o~
the oral composition. The total surface nctive materlal
content of the dentifrice is typically about O.l to 5% by
weight. Preierably about l to 2% by weight of sodium alkyl
sulphate of broad alkyl distribution is present.
The additive which reduces the lump formation,
particularly aging at low temperature, such as about -7 to
7 C., is a water soluble, orally acceptable salt of an alkylene
group contains l-lO carbon atoms. Such salts have the formula:
X20 P-H C / CH2-P
N-(CH2)1l-N
X203P-H2C / ~ CH2-P03X2
wherein n is a number from l to lO and X is hydro~en or
orally acceptable cation such as alkali metal (e.g., sodium
and potassium), ammonium, Cl-Cl8 mono-, di and tri-substituted
ammonium (e.g., mono-, di-, and triethanolammonium salts),
with the proviso that up to 7, preferably 3-5 of the "X"
groups may be hydrogen.
The polyamine polyphosphonic compounds which are most
preferred are water soluble orally acceptable salts (most
preferably tri-, tetra-, or penta-sodium salts of ethylene-
diamine tetra (methylenephosphonic acid), (hereinafter E~ITEMPA.)
Other polyamine polyphosphonic compounds include orally
acceptable water-soluble salts of tetramethylenediamine
tetra (methylenephosphosphonic aclcl), pentam~thylene dlamlne
tetra (methylenephosphonlc acld), hexamethylene
diamine tetra (methylenephosphonic acid) and octamethylene
diamine tetra (methylenephosphonic acid).
The polya~ine polyphosphonate salts thereof can be
prepared in any convenient manner, for example according
to the teachings of U.S. Pat. No. 3',~28,5~6 or Moedritzer
and Irani~ Journal of Organ~c Chemistry, May 1~66, pages
1~03-1607.
The concentration of polyamine polyphosphonates in denti-
frices can range widely 9 typically from about 0.1 to 15% by
weight. Generally, concentrations from about 0.5 to about 5%
by weight are utiliæed.
The opaque dentifrice is typically a toothpaste containing
a gel or liquid vehicle, preferably as a mass of a consistency
which can be extruded from a collapsible tube such as an
aluminum tube or a lead tube. The vehicle contains liquid
and solids. The liquid portion comprises water and generally
a humectant such as glycerine, aqueous sorbitol or polyethylene
glycOl. The total liquid content is at least about 35%,
at least about 35% by weight of the dentifrice being water
(not associated with ht~mectant), typically about 35-50%,
and humectant (including water associated with humectant), if
any, typically about 25-50%, by weight of the dentifrice. The
elevated water content serves to render the dentifrice opaque,
particularly when a polishing agent further to the siliceous
polishing agent is present.
In the liquid portion of the vehcile, sorbitol is suitably
employed as a 70% aqueous solution. Glycerine alone
~:Q ~
or admixed with the sorbltol soLutLon is also a very su:Ltable
humectant.
The solid por~ion of the vehicle is a gelling agent SUCil
as a natural or synthetic gum or gum~ e material, such as
Irish Moss, gum tragacanth, al~ali metal carboxymethyl
cellulose, polyvinyl pyrrolidone, starch, water-soluble
hydrophilic collodial carboxyvinyl polymer such as those
sold as "Carbopol 934" and"Carbopol 940" (CARBOPOL is a trade
mark), and synthetic inorganic silicated clays such as those
sold as "Laponite CP" an~ Laponite SP" ~LAPONITE is a trade
mark). These grade of "Laponite" have the formula
(Si Mg Li O )0.6-Na+ The solid portion of the
vehicle is typcially present in an amount up to 10% of the
dentifrice, preferably from 0.5% to 5%. When employed, grades
of l'Laponite" are preferably used in amounts of from 1% to 5%.
Any suitable flavouring or sweetening materials may be
employed in formulating a flavour for the dentifrices.
Examples of suitable flavouring constituents include flavouring
oils, e.g. oils of spearmint, peppermint, wintergreen,
sassafras, clove, sage, eucalyptus, marjoram, cinnamon, lemon
and orange, as well as methylsalicylate. Suitable sweetening
agents include sucrose, lactose, maltose, sorbitol, dipeptides
as described in U.S. Pat. No. 3,939,261, oxathiazin salts as
described in U.S. Pat. No. 3,932,606, perillartine and saccharine.
Suitably, flavour and sweetening agents may together constitute
from 0.01% to 5% or more of the dentifrice. Chloroform may also
be used.
Various other adjuvant materials may be incorporated in
dentifrlces of this invention. E~amples are pLgments su~h
as titanium dlo~ide and zinc oxlde, preservatives, ællicones
chlorophyll compounds, and ammoniated materials such as urea,
diammonium phospha~e and mixtures thereof. The adjuvants
are incorporat~d in the dentifrices in amounts which do not
substantially adversely affect the properties and characteristics
de8~r~d~
Antibacterial agents may also be employed ln the dentiErice
oE the invention, e.g. in an amount in the range from 0.01%
to 5% by weight. Typical antibacterlal agents include:
N ~(-chlorobenzyl)-N -(2,4-dichlorobenzyl~biguanide;
p-chlorophenyl biguanide;
4-chlorobenzhydryl bigu~lide;
4-chlorobenzylhydrylguanylurea;
N-3-lauroxypropyl-N5-p-chloroben~ylbiguanide;
1,6-di-p-chlorophenylbiguanidohexane;
1,6-bis(2-ethylhexylbiguanido~ hexane;
l-(lauryldimethylammonium)-8-(p-chlorobenzyldimethyl
ammonium) octane dichloride 3
5,6-dichloro-2-guanidinobenzimidaæole;
N -p-chlorophenyl-N5-laurylbiguanide;
5-amino-1,3-bis(2-e~hylhexyl)-5-methylhexahydropyrimidine;
and their non~toxic acid addition salts.
Synthetic finely divided silicas such as those sold as the
"Cab-O-Sil M-5", "Syloid 244", Syloid 266", Aerosil D200" and
mixtures thereof, may also be employed, e.g. in amount of from
0.5% to 20%, to promote thi~kening or gelling (CAB-O-CIL7 SYLOID,
and AEROSIL are trade marks)~
A toothpaste dentifrice may be prepared by forming a gel with
humectant, gum or thickener, sweetener and water and adding
thereto polishing agent, surface active agent, EDITEMPA salt or
the like and flavour. Alternatively the EDITEMPA salt
or the like may be added during gel stage manufacture.
4~
Th~ denttErice should have a pH pr~ctlcable for use
e.g. about 4-10.5~ preferably about 7.5-10.5. The p-l may
be ad~usted with appropriate materials known ln the art, such
as sodium hydro~ide.
The following e~amples -illustrate the ~nvention. All
parts and proportions are by weight unless othe~wise indica~ed.
EXAMPLE 1
The following opaque dentifric~s are prepared and placed
in aluminum tubes having an inner lacquered lining;
PARTS
INGREDIENTS A B
Glycerine 25.00 25.00
Sodium carboxymethyl
cellulose 1.10 1.10
Titanium Dioxide 0.40 0.40
Saccharin acid 0.12 0.12
Silica combined with
alumina (Alusil N - RI 1.45
available from Joseph
Crosfield and Sons, Ltd.
Warrington, England 20.00 20.00
Calcined alumina (MAF-
Microgrit available
from British Aluminum
Company 10. nolo.oo
EDITEMPA Na4-6 salt -- 2.00
Sodium alkyl sulphate
LZV available from Marchon
Division of Albright &
Wilson 1.76 1.76
Flavour 1.20 1.20
Water O.S to 100 Q-S to 100
pH (20~ slurry) io. 2 10.2
Upon extrusion of a ribbon of each dentifrice from the
tube, Dentifrice A has a lumpy surface appearance whilst
Dentifrice B containing salt of EDITEMPA has a rheologically
smooth surface appearance.
11
EXA~LE 2
Similar results to those of Example 1 are obtained when 0.82
parts of sodi~ml n~onofluorophosphate are included in each of dentifrices A
and B. Preferably the wa-ter contents are 40.60 parts and 38.60 parts
respectively ~pH of 20% slurries- A 9.8; B 8.56).
It will be apparent to those skilled in the art that modifications
of the above examples may be made there*o.
- 12 -